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- Tasks: Join us as a Clinical Research Associate, conducting site visits and ensuring compliance in medical research.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work, competitive pay, career growth opportunities, and wellness initiatives.
- Why this job: Make a real impact in healthcare while travelling the UK and working with passionate professionals.
- Qualifications: A bachelor's degree in health or life sciences is preferred; strong communication skills are a plus.
- Other info: Must be willing to travel 60-80% nationally and hold a valid driver's licence.
The predicted salary is between 28800 - 48000 £ per year.
Entry Level – Clinical Research Associate
Join to apply for the Entry Level – Clinical Research Associate role at Medpace
The Clinical Research Associate at Medpace offers an exciting career in drug and medical device development, while making a difference in the lives of others. For those with a medical and/or life science background who wish to explore research, travel the UK, and help bring pharmaceutical and medical devices to market – this could be the right opportunity.
Please note that to take full advantage of the training on offer, you must be within commuting distance of our Medpace central London office as this role is initially fully office based.
Our successful Clinical Research Associates come from varied backgrounds:
- Nurses
- Dieticians
- Pharmacy Technicians
- Pharmaceutical/Device Sales Representatives
- Biotech Engineers
- PhD/Pharm.D candidates
- Health and Wellness Coordinators
- Site Coordinators, Clinical Research Coordinators
- Research Assistants
PACE® – MEDPACE CRA TRAINING PROGRAM
Through our PACE® Training Program, you will join other professionals achieving CRA excellence:
- Provides the platform to effectively and confidently carry out your duties, enhance your current abilities, and help you become a high‑functioning independent Medpace CRA.
- Prepares you by developing CRA skills through interactive discussions, hands‑on job‑related exercises, and practicums.
- Offers core rotations in other clinical research departments to learn aspects of the drug/device development and approval process.
Unexpected Rewards
This role takes you on a journey through travel and excitement, allowing you to make a difference at a large scale. Advantages include:
- Dynamic working environment with varying responsibilities day to day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancement
- Competitive pay and bonus program
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.
- Communicate with the medical site staff, including coordinators, clinical research physicians, and their staff.
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.
- Verify medical record and research source documentation against case report form data; inform site staff of entry errors, ensure good documentation practices, and communicate protocol deviations appropriately per SOPs, GCP and regulatory requirements.
- Verify that the investigator is enrolling only eligible subjects.
- Review regulatory documents.
- Ensure medical device and/or investigational product/drug accountability and inventory.
- Review adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting per protocol.
- Assess the clinical research site’s patient recruitment and retention success and offer suggestions for improvement.
- Complete monitoring reports and follow‑up letters, summarizing significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Qualifications
- Minimum of a bachelor’s degree; health or life science related field preferred.
- Willingness to travel approximately 60‑80% nationally.
- Familiarity with Microsoft Office.
- Strong communication and presentation skills a plus.
- Valid driver’s licence.
- Willingness to be fully office based during the core training program.
Medpace Overview
Medpace is a full‑service clinical contract research organization (CRO) offering Phase I‑IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics with a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral, and anti‑infective areas. Headquartered in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join us today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families facing hundreds of diseases. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO package
- Structured career paths with opportunities for professional growth
- Company‑sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility.
What To Expect Next
A Medpace team member will review your qualifications and, if interested, will contact you with details for the next steps.
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Entry Level - Clinical Research Associate employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry Level - Clinical Research Associate
✨Tip Number 1
Familiarise yourself with the clinical research process and the specific responsibilities of a Clinical Research Associate. Understanding the key tasks, such as monitoring visits and regulatory compliance, will help you speak confidently about your interest in the role during interviews.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry events or join relevant online forums to connect with current Clinical Research Associates. This can provide valuable insights into the role and may even lead to referrals.
✨Tip Number 3
Highlight any relevant experience you have, even if it's not directly related to clinical research. Skills from nursing, pharmacy, or other health-related fields can be very transferable, so be ready to discuss how they apply to the CRA position.
✨Tip Number 4
Prepare for potential travel requirements by ensuring you have a valid driver's licence and are comfortable with the idea of travelling frequently. Being proactive about this aspect can demonstrate your commitment to the role and willingness to meet job expectations.
We think you need these skills to ace Entry Level - Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in health or life sciences. Include any roles that demonstrate your understanding of clinical research, such as internships or volunteer work.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and how your background aligns with the responsibilities of the Clinical Research Associate role. Mention specific skills like communication and attention to detail.
Highlight Relevant Qualifications: Clearly state your educational background, especially if you have a degree in a health or life science field. If you have any certifications or training related to clinical research, be sure to include those as well.
Prepare for Potential Questions: Think about common interview questions related to clinical research and prepare thoughtful responses. Be ready to discuss your understanding of Good Clinical Practice (GCP) and your ability to work in a team.
How to prepare for a job interview at Medpace
✨Know Your Science
Brush up on your knowledge of clinical research and the drug development process. Be prepared to discuss how your background in health or life sciences relates to the role of a Clinical Research Associate.
✨Showcase Your Communication Skills
Since the role involves liaising with medical site staff, demonstrate your strong communication abilities. Prepare examples of how you've effectively communicated complex information in previous roles or studies.
✨Highlight Relevant Experience
Even if you’re entry-level, draw on any relevant experience from internships, volunteer work, or academic projects. Discuss how these experiences have prepared you for the responsibilities outlined in the job description.
✨Ask Insightful Questions
Prepare thoughtful questions about the company culture, training opportunities, and the specifics of the CRA role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.